Sustained circulation of enterovirus D68 in Europe in 2023 and the continued evolution of enterovirus D68 B3-lineages associated with distinct amino acid substitutions in VP1 protein

dc.contributor.authorHirvonen, Aurora
dc.contributor.authorJohannesen, Caroline Klint
dc.contributor.authorSimmonds, Peter
dc.contributor.authorFischer, Thea K.
dc.contributor.authorHarvala, Heli
dc.contributor.authorBenschop, Kimberley S.M.
dc.contributor.authoron behalf of ENPEN study collaborators
dc.contributor.organizationfi=biolääketieteen laitos|en=Institute of Biomedicine|
dc.contributor.organization-code1.2.246.10.2458963.20.77952289591
dc.converis.publication-id491859390
dc.converis.urlhttps://research.utu.fi/converis/portal/Publication/491859390
dc.date.accessioned2025-08-27T22:14:13Z
dc.date.available2025-08-27T22:14:13Z
dc.description.abstract<p><b>Background</b><br></p><p>Enterovirus D68 (EV-D68) causes respiratory disease ranging from mild to severe and in rare cases a paralytic syndrome, called acute flaccid myelitis (AFM). Since the global EV-D68 outbreak in 2014, the virus has mainly circulated in biennial epidemic cycles with peaks detected during even years. However, following the COVID-19 pandemic, the seasonal pattern of EV-D68 has been characterized by large yearly upsurges. Here, we describe the circulation of EV-D68 in Europe in 2023 and track its genetic evolution.<br></p><p><b>Study design</b><br></p><p><b></b>Data was compiled from members of the European Non-Polio Network (ENPEN). This included monthly data on the total number of EV samples tested, EV positive samples, EV-D68 positive samples and cases, and other EV positive samples detected in 2023. Information on sample types and surveillance system was recorded. Sequence data from the VP1 gene was used for phylogenetic and amino acid sequence analysis.<br></p><p><b>Results</b><b></b><br></p><p>EV was detected in 13,585 out of 203,622 diagnostic samples tested (6.7 %), of which 402 (3.0 %) were determined as EV-D68, representing 386 cases. EV-D68 infections peaked in October 2023 (136/386; 35.2 %). 267/386 (69.2 %) of EV-D68 cases were captured through clinical EV surveillance, almost all of which (202/204 of positive samples with sample type information) were detected in respiratory specimens. Phylogenetic analysis performed on 99 VP1 sequences revealed a distinct B3-derived lineage with a previously undescribed residue change, D554E, in Europe.<br></p><p><b>Conclusions</b><br></p><p><b>​​​​​​​</b>The study documents sustained circulation of EV-D68 in Europe in 2023, the evolution of B3-derived lineages, and appearance of previously undescribed amino acid substitutions in Europe. This stresses the need for continuous EV-D68 surveillance and harmonization of EV-D68 detection practices towards better data comparability across countries.<br></p>
dc.identifier.eissn1873-5967
dc.identifier.jour-issn1386-6532
dc.identifier.olddbid201845
dc.identifier.oldhandle10024/184872
dc.identifier.urihttps://www.utupub.fi/handle/11111/50502
dc.identifier.urlhttps://doi.org/10.1016/j.jcv.2025.105785
dc.identifier.urnURN:NBN:fi-fe2025082789587
dc.language.isoen
dc.okm.affiliatedauthorHarvala, Heli
dc.okm.discipline1183 Plant biology, microbiology, virologyen_GB
dc.okm.discipline3111 Biomedicineen_GB
dc.okm.discipline3121 Internal medicineen_GB
dc.okm.discipline1183 Kasvibiologia, mikrobiologia, virologiafi_FI
dc.okm.discipline3111 Biolääketieteetfi_FI
dc.okm.discipline3121 Sisätauditfi_FI
dc.okm.internationalcopublicationinternational co-publication
dc.okm.internationalityInternational publication
dc.okm.typeA1 ScientificArticle
dc.publisherElsevier BV
dc.publisher.countryNetherlandsen_GB
dc.publisher.countryAlankomaatfi_FI
dc.publisher.country-codeNL
dc.relation.articlenumber105785
dc.relation.doi10.1016/j.jcv.2025.105785
dc.relation.ispartofjournalJournal of Clinical Virology
dc.relation.volume178
dc.source.identifierhttps://www.utupub.fi/handle/10024/184872
dc.titleSustained circulation of enterovirus D68 in Europe in 2023 and the continued evolution of enterovirus D68 B3-lineages associated with distinct amino acid substitutions in VP1 protein
dc.year.issued2025

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